Surgical access method and assembly including sleeve and port

ABSTRACT

A surgical access assembly includes a sleeve and a port. The sleeve is adapted for insertion within tissue to access an underlying tissue site. The sleeve defines a first passage therethrough. The first passage has a first diameter. The port defines one or more second passages extending therethrough. The port is adapted for insertion within the first passage of the sleeve in a substantially sealed relationship therewith. The one or more second passages are adapted for a substantially sealed reception of a surgical object therethrough. The one or more second passages have one or more second diameters. The port is selectively removably positionable within the first passage of the sleeve. The first diameter is greater than the one or more second diameters.

CROSS REFERENCE TO RELATED APPLICATION

The present application is a continuation of U.S. application Ser. No. 13/030,178, filed Feb. 18, 2011, which claims the benefit of U.S. Provisional Application Ser. No. 61/323,102 filed on Apr. 12, 2010, the entire contents of each of which are incorporated herein by reference.

BACKGROUND

1. Technical Field

The present disclosure relates generally to a surgical access assembly and method for use in minimally invasive surgical procedures, such as endoscopic or laparoscopic type procedures, and more particularly to a surgical access method and assembly including a sleeve and port for providing access to a body cavity.

2. Background of Related Art

Today, many surgical procedures are performed through small incisions in the skin, as compared to the larger incisions typically required in traditional procedures, in an effort to reduce both trauma to the patient and recovery time. Generally, such procedures are referred to as “endoscopic”, unless performed on the patient's abdomen, in which case the procedure is referred to as “laparoscopic”. Throughout the present disclosure, the term “minimally invasive” should be understood to encompass both endoscopic and laparoscopic procedures.

During a typical minimally invasive procedure, surgical objects, such as surgical access devices (e.g., trocar and cannula assemblies) or endoscopes, are inserted into the patient's body through the incision in tissue. In general, prior to the introduction of the surgical object into the patient's body, insufflation gases are used to enlarge the area surrounding the target surgical site to create a larger, more accessible work area. Accordingly, the maintenance of a substantially fluid-tight seal is desirable so as to prevent the escape of the insufflation gases and the deflation or collapse of the enlarged surgical site.

To this end, various access devices with valves and seals are used during the course of minimally invasive procedures and are widely known in the art. However, a continuing need exists for surgical access devices that can facilitate the accessibility of an underlying tissue site with relative ease and with minor inconvenience for the surgeon.

SUMMARY

The present disclosure is directed to a surgical access assembly that includes a sleeve and a port. The sleeve includes a sleeve body having first and second ends. The sleeve body may be formed of a flexible material and the first and second ends may be formed of one or more of a rigid and a semi-rigid material. The sleeve is adapted for insertion within tissue to access an underlying tissue site. The sleeve defines a first passage therethrough. The first passage permits unsealed access to the underlying tissue site. The first passage has a first diameter.

The port defines one or more second passages extending therethrough. The port is adapted for insertion within the first passage of the sleeve in a substantially sealed relationship therewith. The one or more second passages are adapted for a substantially sealed reception of a surgical object therethrough. The one or more second passages have one or more second diameters. The port is selectively removably positionable within the first passage of the sleeve. The first diameter is greater than the one or more second diameters. One or both of the sleeve and the port may be substantially hourglass-shaped.

In embodiments, one or more clamps may operably couple the sleeve and the port. The one or more clamps are repositionable between clamped and unclamped configurations. The one or more clamps may include one or more locking elements. The one or more locking elements are adapted to lock the sleeve and the port together when positioned in the clamped configuration.

In one aspect, the present disclosure is directed to a method of accessing an underlying tissue site. The method includes providing a surgical access assembly that includes a sleeve and a port. The sleeve defines a first passage therethrough. The first passage has a first diameter. The port defines one or more second passages extending therethrough. The one or more second passages define one or more second diameters. The one or more second diameters are smaller than the first diameter. The method includes selectively positioning the sleeve in an incision or a natural orifice of a patient; selectively positioning the port within the first passage of the sleeve; and selectively accessing the underlying tissue site through one or more of the first passage and the one or more second passages. The method may include advancing a surgical object through the one or more second passages in a substantially sealed relationship therewith. In one respect, the method includes selectively removing the port from the sleeve. In another respect, the method may include inserting the sleeve within a Hasson incision. The method may include inserting the sleeve within a patient to access the colon. The method may include coupling the sleeve and the port with a clamp so that the sleeve and port are in a locked position relative to one another. In one respect, the method includes withdrawing a specimen through the first passage of the sleeve.

BRIEF DESCRIPTION OF THE DRAWINGS

Various embodiments of the present disclosure are described hereinbelow with reference to the drawings, wherein:

FIG. 1 is an exploded, cross-sectional view, with parts separated, of one embodiment of a surgical access assembly in accordance with the present disclosure;

FIG. 2 is a top plan view of one embodiment of a clamp in accordance with the present disclosure;

FIG. 3 is a cross-sectional view of the surgical access assembly of FIG. 1 shown positioned within tissue;

FIG. 4 is a side view of another embodiment of a surgical access assembly with a plurality of instruments shown positioned therein in accordance with the present disclosure; and

FIG. 5 is a top, perspective view of the surgical access assembly of FIG. 4 with the plurality of instruments shown positioned therein.

DETAILED DESCRIPTION OF EMBODIMENTS

Particular embodiments of the present disclosure will be described herein with reference to the accompanying drawings. As shown in the drawings and as described throughout the following description, and as is traditional when referring to relative positioning on an object, the term “proximal” or “trailing” refers to the end of the apparatus that is closer to the user and the term “distal” or “leading” refers to the end of the apparatus that is farther from the user. In the following description, well-known functions or constructions are not described in detail to avoid obscuring the present disclosure in unnecessary detail.

One type of minimal invasive surgery described herein is multiple instrument access through a single surgical port. This technique is a minimally invasive surgical procedure, which permits a surgeon to operate through a single entry point, typically the patient's navel. The disclosed procedure involves insufflating the body cavity and positioning a housing member within an opening in the patient's skin (e.g., an incision or a naturally occurring orifice). Instruments including an endoscope and additional instruments such as graspers, staplers, forceps or the like may be introduced within the port to carry out the surgical procedure.

Referring now to the drawings, in which like reference numerals identify identical or substantially similar parts throughout the several views, FIG. 1 illustrates a surgical access assembly 100 that includes a sleeve 110 and a port 120. The sleeve 110 includes a sleeve body 112 having first and second ends 112 a, 112 b on respective proximal and distal ends of the sleeve body 112 that are integrally formed with the sleeve body 112. The sleeve body 112 may be formed of a flexible material, e.g., elastomeric material such as rubber or any other suitable material in order to conform to the tissue tract “TT” (FIG. 3) of an incision or natural orifice. Alternatively, the sleeve body 112 may be formed of an inflexible material and may conform to the tissue tract “TT” (FIG. 3) of an incision or natural orifice by virtue of a biasing force of the port, as will be explained further below.

In embodiments, the first and second ends 112 a, 112 b, which may be annular rings 112 a, 112 b, may be formed of a rigid and/or a semi-rigid material, e.g., a polymeric material or any other suitable material. For example, the first and second ends 112 a, 112 b may include annular rings 112 a, 112 b that are formed of a material that is semi-rigid such that the leading annular ring 112 b may be deformed for insertion into an incision or opening in the body, and that is resiliently biased towards its initial position so as to retain the sleeve within the incision or opening once placed therewithin. In addition, the first end 112 a may include an annular ring that is formed of a material that is semi-rigid such that the trailing annular ring may be, e.g., rolled, over the sleeve 112 in order to retract the incision before during or after insertion of the port therewithin. The first ring 112 a may have any number of different shapes, e.g., cross-sectional shapes, for, e.g., providing gripping surfaces to a user, for improving the ability of the sleeve to resist un-rolling, to improve the ability of the ring to be rolled. Alternatively, a simple ring 112 a having a circular or substantially circular cross-section may be employed.

As best shown in FIG. 3, the sleeve 110 is adapted for insertion within tissue “T” to access an underlying tissue site “TS”, e.g., through the abdominal or peritoneal lining in connection with a laparoscopic surgical procedure. The sleeve 110 defines a first passage 114 therethrough. The first passage 114 permits unsealed access to the underlying tissue site “TS.” The first passage 114 has a first diameter that is adapted to accommodate the port 120 therein.

The port 120 defines one or more second passages 122 extending therethrough. One type of port that may be employed is disclosed and illustrated in Applicant's U.S. Provisional Patent Appl. Ser. No. 60/997,885, filed Oct. 5, 2007, the entire contents of which are hereby incorporated by reference herein. The port 120 is adapted for insertion within the first passage 114 of the sleeve 110 in a substantially sealed relationship therewith when sleeve 110 is inserted through an opening in tissue “T”. The one or more second passages 122 are adapted for a substantially sealed reception of a surgical object “I” (FIGS. 4 and 5) therethrough, e.g., a cannula or other type of surgical instrument. The one or more second passages 122 may have one or more second diameters in order to accommodate variously-sized surgical objects “I” (FIGS. 4 and 5) in a substantially sealed relationship therewith. The first diameter is greater than the one or more second diameters so that the port 120 can be selectively removably positioned within the first passage 114 of the sleeve 110. The port 120 may be made from a disposable, compressible, and/or flexible type material such as a suitable foam or gel material having sufficient compliance to form a seal about one or more surgical objects “I” (FIGS. 4 and 5). The foam is preferably sufficiently compliant to accommodate off axis motion of the surgical object. In one embodiment, the foam includes a polyisoprene material. In embodiments, the material may be elastomeric.

Referring now to FIGS. 2 and 3, one or more clamps 130 may operably couple the sleeve 110 and the port 120. The one or more clamps 130 are repositionable between clamped (FIG. 3) and unclamped (FIG. 2) configurations. As shown in FIG. 2, the one or more clamps 130 may include one or more locking elements 132, e.g., a screw “S” and nut “N” and first and second sections 130 a, 130 b. With reference to FIG. 3, the one or more locking elements 132 are adapted to lock the sleeve 110 and the port 120 together when positioned in the clamped configuration. In particular, the screw “S” may be tightened through screw holes (not shown) defined within each of the first and second sections 130 a, 130 b until the sleeve body 112 is secured to the port 120. As best shown in FIG. 3, the first and second sections 130 a, 130 b may be adapted to be secured within a channel 126 defined about the circumference of the port 120 between upper and lower lips 124 a, 124 b thereof.

In use of the surgical access assemblies 100, the sleeve 110, 210 is selectively positioned to a predetermined depth in an incision, e.g., a navel incision or a Hasson incision, or a natural orifice of a patient, which may include the anus and the vagina in order to selectively access the underlying tissue site “TS” (e.g., colon, uterus, etc.) through the first passage 114. The port 120 may then be selectively positioned within the first passage 114 of the sleeve 110 in order to selectively access the underlying tissue site “TS” through the one or more second passages 122. In the embodiment shown in FIGS. 1-3, the port 120 is configured to be positioned outside of the incision (see FIG. 3), such that the distal face of the port 120 rests against the outer wall of the patient's body. As illustrated in FIG. 3, the clamp 130 may then be used to couple the sleeve 110 and the port 120 so that the sleeve 110, 210 and the port 120, 220 are in a locked position relative to one another. A surgical object “I” may then be advanced through the one or more second passages 122 in a substantially sealed relationship therewith, and where necessary, insufflation fluid, e.g., CO₂, may be introduced into the underlying tissue site “TS” with one or more of the surgical objects “I” in order to create a working space in the underlying tissue site “TS.” Should the clinician need to access the underlying tissue site “TS” through a larger diameter, e.g., to remove a specimen therefrom, the clinician may then readily selectively disconnect the clamp 130 and remove the port 120 from the sleeve 110 to gain access again through the first passage 114.

As illustrated in FIGS. 4 and 5, one embodiment of a surgical access assembly is generally designated as 200. In this embodiment, the surgical access assembly 200 includes a sleeve 210 and a port 220. The sleeve 210 includes a sleeve body 212 having first and second ends 212 a, 212 b on respective proximal and distal ends of the sleeve body 212 that are integrally formed with, or otherwise connected to, the sleeve body 212. One or both of the sleeve 210 and the port 220 may be substantially hourglass-shaped. Alternatively, the port 220 may be hourglass-shaped while the sleeve 212 may be generally cylindrical when in an inoperative position.

In use of the surgical access assemblies 200, the sleeve 210 is selectively positioned to a predetermined depth in an incision, e.g., a navel incision or a Hasson incision, or a natural orifice of a patient, which may include the anus and the vagina in order to selectively access the underlying tissue site “TS” (e.g., colon, uterus, etc.) through the first passage 114. The port 220 may then be selectively positioned within the first passage 114 of the sleeve 110, 210 in order to selectively access the underlying tissue site “TS” through the one or more second passages 122. Unlike the embodiment shown in FIGS. 1-3, in which the clamp 130 is used to couple the sleeve 110 and the port 120 so that the sleeve 110 and the port 120 are in a locked position relative to one another, in this embodiment, the port 220 is maintained in position by the biasing force of the port 220 expanding outwardly after being compressed to fit within the incision or opening. More specifically, in the absence of the incision or opening, the port 220 is not securely attached or fixed in any way relative to the sleeve 210, but rather is completely free to move relative to the sleeve 210. The sleeve 210 does not engage the port 220, but rather is trapped between the wall of the incision or opening and the sidewall of the flexible port. Advantageously, the port 220 is dimensioned so as to extend fully through the thickness of the patient's incision or opening, e.g., such that the upper portion of the port 220 is positioned above the outer wall of the incision or opening, the middle region of the port 220 is positioned within the incision or opening, and the lower portion of the port 220 is positioned below the lower wall of the incision or opening, thereby insuring that the port 220 will be maintained in position within the incision or opening and provide adequate sealing at all locations within the incision or opening. A surgical object “I” may then be advanced through the one or more second passages 122 in a substantially sealed relationship therewith, and where necessary, insufflation fluid, e.g., CO₂, may be introduced into the underlying tissue site “TS” with one or more of the surgical objects “I” in order to create a working space in the underlying tissue site “TS.” Should the clinician need to access the underlying tissue site “TS” through a larger diameter, e.g., to remove a specimen therefrom, the clinician may then readily selectively remove the port 220 from the sleeve 210, to gain access again through the first passage 114. In addition, if desired, the clinician may then replace the port 220 within the sleeve 210 and continue with other aspects of the surgical procedure with the port 220 in place in the sleeve 210 and within the incision or opening.

In embodiments of the present disclosure, surgical access assemblies 100, 200 may come preassembled with the port 120, 220 disposed within the sleeve 110, 210. In the alternative, the port 120, 220 may be positioned within sleeve 110, 210 at the surgical site as discussed above.

Although the illustrative embodiments of the present disclosure have been described herein with reference to the accompanying drawings, the above description, disclosure, and figures should not be construed as limiting, but merely as exemplifications of particular embodiments. It is to be understood, therefore, that the disclosure is not limited to those precise embodiments, and that various other changes and modifications may be effected therein by one skilled in the art without departing from the scope or spirit of the disclosure. 

The invention claimed is:
 1. A surgical access device, comprising: a wound retractor having a sleeve with a distal end and a proximal end, the distal end of the sleeve attached to a distal ring for insertion through an incision and configured to be maintained internally relative to a body cavity during use, the proximal end of the sleeve attached to a proximal ring that is configured to be maintained externally relative to the body cavity during use, the proximal ring being rollable so as to shorten a longitudinal length of the sleeve to thereby cause the sleeve to retract tissue that forms the incision; and a flexible port having an outer surface, the flexible port defining at least one opening therethrough for sealed reception of a surgical object, wherein the flexible port is configured to be compressed by a compressive force into a compressed condition in which the flexible port may be inserted into the retracted incision, and when the compressive force is removed, the flexible port expands such that the outer surface of the flexible port presses against and forms a seal with the tissue that forms the incision, the sleeve of the wound retractor being sandwiched between the outer surface of the flexible port and the tissue, the flexible port including proximal and distal ends, the proximal end of the flexible port having an upper lip and the distal end of the flexible port having a lower lip, the upper lip positionable above an upper surface of the tissue and the lower lip positionable below a lower surface of the tissue such that the proximal and distal ends of the flexible port are positionable between the proximal and distal ends of the sleeve, wherein the flexible port is maintained between the proximal and distal ends of the sleeve by a biasing force exerted by the flexible port on the sleeve.
 2. The surgical access device of claim 1, wherein the outer surface of the flexible port has an hourglass shape.
 3. The surgical access device of claim 1, wherein the upper lip of the flexible port is configured to be maintained externally relative to the body cavity during use.
 4. The surgical access device of claim 1, wherein the lower lip of the flexible port is configured to be maintained internally relative to the body cavity during use.
 5. The surgical access device of claim 1, wherein the flexible port is made of foam.
 6. The surgical access device of claim 1, wherein the flexible port defines a plurality of openings therethrough for sealed reception of surgical objects.
 7. The surgical access device of claim 1, wherein the at least one opening defined by the flexible port is configured for sealed reception of a trocar cannula.
 8. The surgical access device of claim 1, further including a trocar cannula configured for sealed reception in the at least one opening defined by the flexible port. 